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rs794727123

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794727123(A;A)
Make rs794727123(A;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position32573744
GeneDMD
is asnp
is mentioned by
dbSNPrs794727123
ebirs794727123
HLIrs794727123
Exacrs794727123
Varsomers794727123
Maprs794727123
PheGenIrs794727123
hapmaprs794727123
1000 genomesrs794727123
hgdprs794727123
ensemblrs794727123
gopubmedrs794727123
geneviewrs794727123
scholarrs794727123
googlers794727123
pharmgkbrs794727123
gwascentralrs794727123
openSNPrs794727123
23andMers794727123
23andMe allrs794727123
SNP Nexus

SNPshotrs794727123
SNPdbers794727123
MSV3drs794727123
GWAS Ctlgrs794727123
Max Magnitude0
ClinVar
Risk rs794727123(A;A)
Alt rs794727123(A;A)
Reference rs794727123(G;G)
Significance Pathogenic
Disease Becker muscular dystrophy Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Becker muscular dystrophy Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32591861C>T
CLNSRC
CLNACC RCV000174742.1, RCV000174743.1,